skip to Main Content

Ledige stillinger

Du er velkommen til at sende en uopfordret ansøgning også

Compliance consultant

Do you want to be part of a strong team in a growing company?

We are currently seeking an experienced and dedicated Compliance Consultant.

 Description:

This person will be responsible for:

  • Creating computer system validation (CSV) deliverables (Validation Plans, Requirements, Design Specs, Test Scripts (IQ / OQ / PQ), Summary Reports, Trace Matrices, SOPs)
  • Execute validation test plans and document results in e.g. HP ALM
  • Perform validation activities in GxP systems (e.g. ARISg, LIMS, SAP, QMS)
  • Perform work in Quality Management System (QMS) records (e.g. Deviations, CAPAs, Change Management)

 Requirements  

  • 5 – 7 years’ experience validating GxP systems within the pharmaceutical, biotech, or medical device fields
  • Able to create computer system validation (CSV) deliverables (Validation Plans, Requirements, Design Specs, Test Scripts (IQ / OQ / PQ), Summary Reports, Trace Matrices, SOPs)
  • Familiar with one or more of the following types of systems: HP ALM, ARISg, LIMS, QMS or SAP
  • Working experience with Quality Management System (QMS) records (e.g. Deviations, CAPAs, Change Management)
  • Able to understand current work processes and suggest process improvements
  • Able to work both as part of a team and independently
  • Ability to work daily on-premise in Denmark/Copenhagen
  • Excellent English and preferable also Danish communication skills (verbal, written)

Please sent your motivated application and resume to marianne@convergingminds.dk

Back To Top